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Exact(14)
Paclitaxel responses in relation to individual mutations are presented in Supporting Information Table S1.
Mutations are presented as an italicized superscript (e.g., rtls l1 ).
Meanwhile, top seven hereditary retinal diseases with the highest number of related mutations are presented.
Details of SCN1A mutations are presented in the Supplementary Tables 3 and 4.
All CEBPA mutations are presented in detail in Supplementary Tables S2A and S2B.
Reported IC50 values of clinically detected mutations are presented in Table 2 >.
Similar(46)
Summary of cell line mutations is presented in Supplementary Table 1.
Five cases with rare mutations and one case with novel mutation are presented in Table 2.
The genotypes for marker FCA931 and for the mutation are presented in Fig. 1.
In Fig. 5c, an example of mutation is presented.
Genetic testing involves looking at a person's DNA to see if certain mutations are present.
More suggestions(15)
mutations are preferred
mutations are proposed
deployment are presented
transfer are presented
mutations are summarized
mutations are associated
mutations are known
mutations are seen
mutations are observed
mutations are spread
mutations are detected
mutations are mapped
mutations are kept
mutations are located
mutations are replicated
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